What are the responsibilities and job description for the PharmaSuite MES Author position at Largeton Group?
Job Summary (PharmaSuite MES Author)
- Lead the design, development, documentation, and implementation of Rockwell FactoryTalk PharmaSuite (FTPS) MES solutions.
- Design, author, develop, and configure Electronic Batch Records (EBR).
- Implement MES solutions and integrate them with ERP and control systems.
- Document MES configurations and validate EBRs to ensure compliance.
- Collaborate with business management and end-users to define requirements and deliver value-added solutions.
- Document and analyze business information needs and ensure solutions meet GxP and regulatory standards.
- Prepare and respond to client proposals as required.
- Manage and develop client relationships to support project success.
- Ensure all solutions adhere to FDA and GMP guidelines.
- Apply understanding of Life Sciences validation processes and SDLC/support methodologies.
- Travel up to 100% as needed for client site visits and project delivery.
- Minimum requirements: 5 years’ work experience, 1 year with Rockwell FTPS MES in Life Sciences manufacturing, and a High School Diploma or GED.
